Canonical Allele Identifier: CA2607166
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs760667657

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530982C>T , CM000665.2:g.129530982C>T GRCh38
NC_000003.11:g.129249825C>T , CM000665.1:g.129249825C>T GRCh37
NC_000003.10:g.130732515C>T NCBI36
NG_009115.1:g.7344C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.468C>T MANE Select ENSP00000296271.3:p.Gly156=
ENST00000296271.3:c.468C>T ENSP00000296271.3:p.Gly156=
NM_000539.3:c.468C>T MANE Select NP_000530.1:p.Gly156=